Effectiveness of Egg Versus Whey Protein Powder During Resistance Training

May 24, 2024 updated by: Phil Chilibeck, University of Saskatchewan

Egg Versus Whey Protein as the Optimal Supplement for Fitness-conscious People

Consumption of whole eggs has recently been shown to stimulate muscle protein synthesis to a greater degree than consumption of egg whites after a resistance training session. It is theorized that the egg yoke contains bio-active nutrients that enhance the protein provided by egg whites. The study will evaluate the effect of whole egg powder compared to whey protein powder and placebo over 12 weeks of resistance training in men and women who are participating in resistance training programs.

Study Overview

Detailed Description

Consuming whole eggs after resistance training sessions appears to be more effective for simulating muscle protein synthesis that simply consuming egg whites. The egg yolks might enhance the effect of protein derived from egg whites. The study will compare post-exercise supplementation with about 30 grams of protein derived from whole egg powder versus whey protein powder and placebo (maltodextrin) over a 12-week resistance training program. Resistance-trained men and women (n=120) will be randomized to consume either the whole-egg powder, whey protein powder or maltodextrin after resistance training 6 times per week for 12 weeks. The primary outcome measure is change in lean tissue mass. Secondary measures include change in fat mass, change in arm and leg muscle thickness, change in bench press, squat, and knee extension strength, and change in fasting blood glucose.

Study Type

Interventional

Enrollment (Actual)

115

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Saskatchewan
      • Regina, Saskatchewan, Canada, S4S 0A2
        • University of Regina
      • Saskatoon, Saskatchewan, Canada, S7N5B2
        • University of Saskatchewan

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Resistance training experience for at least one year

Exclusion Criteria:

  • Having taken any nutritional supplements the past 30 days
  • Currently using anabolic steroids
  • Currently taking corticosteroids
  • Allergies to dairy or egg products
  • Identifying any medical conditions as determined by the "Get Active Questionnaire"

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Whole egg powder
Dietary supplementation with whole egg powder after resistance training sessions
Nutritional supplementation during a 12 week resistance training program
Active Comparator: Whey protein powder
Dietary supplementation with whey protein powder after resistance training sessions
Nutritional supplementation during a 12 week resistance training program
Placebo Comparator: Maltodextrin placebo
Dietary supplementation with maltodextrin placebo after resistance training sessions
Nutritional supplementation during a 12 week resistance training program

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in lean tissue mass
Time Frame: 12 weeks
Lean tissue mass measured by DXA
12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in fat mass
Time Frame: 12 weeks
Fat mass measured by DXA
12 weeks
Change in biceps muscle thickness
Time Frame: 12 weeks
biceps muscle thickness measured by ultrasound
12 weeks
Change in triceps muscle thickness
Time Frame: 12 weeks
triceps muscle thickness measured by ultrasound
12 weeks
Change in quadriceps muscle thickness
Time Frame: 12 weeks
quadriceps muscle thickness measured by ultrasound
12 weeks
Change in hamstrings muscle thickness
Time Frame: 12 weeks
hamstrings muscle thickness measured by ultrasound
12 weeks
Change in bench press strength
Time Frame: 12 weeks
Bench press strength (kg)
12 weeks
Change in leg squat strength
Time Frame: 12 weeks
Leg squat strength (kg)
12 weeks
Change in knee extension strength
Time Frame: 12 weeks
Isokinetic knee extension torque
12 weeks
Change in fasting glucose
Time Frame: 12 weeks
Fasting glucose
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Philip Chilibeck, Ph.D., University of Saskatchewan
  • Principal Investigator: Darren Candow, Ph.D., University of Regina

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 30, 2022

Primary Completion (Actual)

August 31, 2023

Study Completion (Actual)

August 31, 2023

Study Registration Dates

First Submitted

January 11, 2022

First Submitted That Met QC Criteria

January 11, 2022

First Posted (Actual)

January 25, 2022

Study Record Updates

Last Update Posted (Actual)

May 29, 2024

Last Update Submitted That Met QC Criteria

May 24, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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